Literature DB >> 19515446

In vitro and in vivo safety evaluation of the bacteriocin producer Streptococcus macedonicus ACA-DC 198.

Petros A Maragkoudakis1, Marina Papadelli, Marina Georgalaki, Effie G Panayotopoulou, Beatriz Martinez-Gonzalez, Andreas F Mentis, Kalliopi Petraki, Dionyssios N Sgouras, Effie Tsakalidou.   

Abstract

Streptococcus macedonicus ACA-DC 198, a bacteriocin producer isolated from Greek Kasseri cheese, was used in a series of in vitro and in vivo experiments in order to evaluate its pathogenic potential. The strain was examined in vitro for haemolytic activity, antibiotic resistance and presence of pathogenicity genes encountered in Streptococcus pyogenes. Subsequently, the strain was orally administered to mice (8.9 log cfu daily), continuously over a period of 12 weeks, in order to ascertain the effects of its long term consumption on animal health and gastric inflammation. S. macedonicus ACA-DC 198 was found to be non-haemolytic and sensitive to ampicillin, chloramphenicol, ciprofloxacin, erythromycin, streptomycin, tetracycline, and vancomycin, with the only resistance observed against kanamycin. PCR amplification and DNA-DNA hybridization did not reveal the presence of any of the S.pyogenes pathogenicity genes examined, namely emm, scpA, hasA, speB, smez2, speJ, sagAB, hylA, ska, speF, speG, slo, hylP2 and mga. In the mouse study, no detrimental effects were observed in the behaviour, general well being, weight gain and water consumption of the animals receiving S. macedonicus ACA-DC 198. Histologic analysis showed no evidence of inflammation in the stomach of the animals receiving S. macedonicus ACA-DC 198, while faecal microbiological analysis revealed that the strain retained its viability passing through the mouse gastrointestinal tract. Finally, no evidence of translocation to the liver, spleen and mesenteric lymph nodes was observed. In conclusion, none of the examined virulence determinants were detected in S. macedonicus ACA-DC 198 and its long term, high dosage oral administration did not appear to induce any pathogenic effect in mice.

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Year:  2009        PMID: 19515446     DOI: 10.1016/j.ijfoodmicro.2009.05.012

Source DB:  PubMed          Journal:  Int J Food Microbiol        ISSN: 0168-1605            Impact factor:   5.277


  7 in total

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Journal:  Braz J Microbiol       Date:  2018-12-04       Impact factor: 2.476

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Journal:  Appl Environ Microbiol       Date:  2010-04-23       Impact factor: 4.792

3.  Postbiotic and Anti-aflatoxigenic Capabilities of Lactobacillus kunkeei as the Potential Probiotic LAB Isolated from the Natural Honey.

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Journal:  Probiotics Antimicrob Proteins       Date:  2021-04       Impact factor: 4.609

4.  Comparative genomics of the dairy isolate Streptococcus macedonicus ACA-DC 198 against related members of the Streptococcus bovis/Streptococcus equinus complex.

Authors:  Konstantinos Papadimitriou; Rania Anastasiou; Eleni Mavrogonatou; Jochen Blom; Nikos C Papandreou; Stavros J Hamodrakas; Stéphanie Ferreira; Pierre Renault; Philip Supply; Bruno Pot; Effie Tsakalidou
Journal:  BMC Genomics       Date:  2014-04-08       Impact factor: 3.969

5.  Acquisition through horizontal gene transfer of plasmid pSMA198 by Streptococcus macedonicus ACA-DC 198 points towards the dairy origin of the species.

Authors:  Konstantinos Papadimitriou; Rania Anastasiou; Eleni Maistrou; Thomas Plakas; Nikos C Papandreou; Stavros J Hamodrakas; Stéphanie Ferreira; Philip Supply; Pierre Renault; Bruno Pot; Effie Tsakalidou
Journal:  PLoS One       Date:  2015-01-13       Impact factor: 3.240

6.  Effects of artificial honey and epigallocatechin-3-gallate on streptococcus pyogenes.

Authors:  Song Chen; Ruijie Huang; Xiaoge Jiang; An Lin; Shijia Li; Yangyang Shi; Fangjie Zhou; Grace Gomez Felix Gomez; Richard L Gregory; Chaoliang Zhang
Journal:  BMC Microbiol       Date:  2022-08-26       Impact factor: 4.465

7.  Comparative genome analysis of Streptococcus infantarius subsp. infantarius CJ18, an African fermented camel milk isolate with adaptations to dairy environment.

Authors:  Christoph Jans; Rainer Follador; Mira Hochstrasser; Christophe Lacroix; Leo Meile; Marc J A Stevens
Journal:  BMC Genomics       Date:  2013-03-22       Impact factor: 3.969

  7 in total

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